Royle N J, Clarkson R E, Wong Z, Jeffreys A J
Department of Genetics, University of Leicester, United Kingdom.
Genomics. 1988 Nov;3(4):352-60. doi: 10.1016/0888-7543(88)90127-9.
Six of the human minisatellites detected by DNA fingerprint probes have been localized by in situ hybridization to human metaphase chromosomes. These hypervariable loci are not dispersed at random in the human genome, but show preferential, though not exclusive, localization to terminal G-bands of human autosomes. Two of the proterminal minisatellites are very closely linked to other variable loci. Sequence analysis of one of these additional minisatellites suggests that the two linked minisatellites arose by independent amplification of different repeat units. The proterminal regions of human autosomes may therefore be rich in minisatellites, analogous to the pseudoautosomal terminal pairing region of human sex chromosomes that is similarly abundant in hypervariable minisatellites.
通过DNA指纹探针检测到的6个人类小卫星已通过原位杂交定位到人类中期染色体上。这些高变位点在人类基因组中并非随机分布,而是优先(但不唯一)定位到人类常染色体的末端G带。两个近端小卫星与其他可变位点紧密连锁。对其中一个额外小卫星的序列分析表明,这两个连锁的小卫星是由不同重复单元的独立扩增产生的。因此,人类常染色体的近端区域可能富含小卫星,类似于人类性染色体的假常染色体末端配对区域,该区域同样富含高变小卫星。